Taiwan FDA registration a0bb0a516aa476c30d0a4c376fe81f6b

"Baxter" gram coagulation spray catheter set

TW: “百特”克滲凝噴霧導管套組

Taiwan·Risk Class 2·Made (部分製程) in POLAND;; Baxter Healthcare SA;; Baxter S.A.·Registered Dec 07, 2009 – Dec 07, 2029Active

Registration details

Analysis ID: a0bb0a516aa476c30d0a4c376fe81f6b
Customs Code: DHA00602046707

Company information

Manufacturer: Made (部分製程) in POLAND;; Baxter Healthcare SA;; Baxter S.A.
Manufacturer Country: Belgium;;Switzerland;;Poland
Authorized Representative: BAXTER HEALTHCARE LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5860 活塞式注射筒
Import Information: import

Dates and status

Registration Date: Dec 07, 2009
Expiry Date: Dec 07, 2029

About this record

Access comprehensive regulatory information for "Baxter" gram coagulation spray catheter set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0bb0a516aa476c30d0a4c376fe81f6b and manufactured by Made (部分製程) in POLAND;; Baxter Healthcare SA;; Baxter S.A.. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..

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